FDA Adverse Event Injury Summary report: N

LIBERTY CYCLER SET, DUAL PATIENT CONNECT

MDR report key: 3810650 · Received April 30, 2014

Report

Report Number
8030665-2014-00339
Event Type
Injury
Date Received
April 30, 2014
Date of Event
April 1, 2014
Report Date
April 29, 2014
Manufacturer
FRESENIUS MEDICAL CARE NORTH AMERICA
Product Code
FKX
PMA / PMN Number
K043363
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Occupation
PATIENT

Narratives

Additional Manufacturer Narrative · 1

A SUPPLEMENTAL REPORT WILL BE SUBMITTED UPON FINAL REVIEW OF MEDICAL RECORDS BY POST MARKET CLINICAL PHYSICIAN AND COMPLETION OF THE PLANT'S INVESTIGATION. RELATED MDRS: 2937457-2014-00733 AND 1713747-2014-99954.

Description of Event or Problem · 1

A PERITONEAL DIALYSIS (PD) PATIENT REPORTED AIR BUBBLES GOING INTO HIS MACHINE AND LATER FEELING FULL. THE PATIENT WAS TREATED WITH PROPHYLACTIC ANTIBIOTICS. THE PATIENT THEN WENT ON TO DEVELOP CONFIRMED PROVIDENCIA RETTGERI PERITONITIS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
258772 LIBERTY CYCLER SET, DUAL PATIENT CONNECT FKX FRESENIUS MEDICAL CARE NORTH AMERICA 13NR08054

Patients

Seq Age Sex Outcome Treatment
1 19 YR Required Intervention LIBERTY CYCLER, DELFLEX PD SOLUTIONS